List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 1A by Illumina Laboratory Services, Illumina

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Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_004004.6(GJB2):c.-6T>A	rs148136545	0.00355
NM_004004.6(GJB2):c.*786G>A	rs187158699	0.00347
NM_004004.6(GJB2):c.*1016A>G	rs537683957	0.00158
NM_004004.6(GJB2):c.*3C>A	rs111033460	0.00155
NM_004004.6(GJB2):c.*115A>C	rs557953001	0.00058
NM_004004.6(GJB2):c.-22-6T>C	rs141962118	0.00044
NM_004004.6(GJB2):c.*423C>T	rs112457424	0.00029
NM_004004.6(GJB2):c.*598C>A	rs550600399	0.00029
NM_004004.6(GJB2):c.*1033G>A	rs185790172	0.00026
NM_004004.6(GJB2):c.*114T>C	rs182085649	0.00012
NM_004004.6(GJB2):c.*800A>G	rs886050027	0.00011
NM_004004.6(GJB2):c.37G>A (p.Val13Met)	rs768130937	0.00010
NM_004004.6(GJB2):c.-1G>A	rs768338285	0.00006
NM_004004.6(GJB2):c.*1040A>G	rs1370756376	0.00004
NM_004004.6(GJB2):c.*236A>T	rs922232025	0.00004
NM_004004.6(GJB2):c.*308G>A	rs886090162	0.00004
NM_004004.6(GJB2):c.287C>G (p.Ala96Gly)	rs201839979	0.00003
NM_004004.6(GJB2):c.510C>T (p.Asn170=)	rs763068053	0.00002
NM_004004.6(GJB2):c.*550A>G	rs1959051090	0.00001
NM_004004.6(GJB2):c.*679T>C	rs1006432105	0.00001
NM_004004.6(GJB2):c.*979A>G	rs546826225	0.00001
NM_004004.6(GJB2):c.174A>G (p.Pro58=)	rs778922005	0.00001
NM_004004.6(GJB2):c.196G>A (p.Asp66Asn)	rs104894403	0.00001
NM_004004.6(GJB2):c.557C>T (p.Thr186Met)	rs753674300	0.00001
NM_004004.6(GJB2):c.60T>G (p.Ile20Met)	rs749693224	0.00001
NM_004004.6(GJB2):c.*1206T>G	rs886050026
NM_004004.6(GJB2):c.*385G>C	rs1959052059
NM_004004.6(GJB2):c.*412A>C	rs547859391
NM_004004.6(GJB2):c.*482A>G	rs886050028
NM_004004.6(GJB2):c.*52C>T	rs1959054328
NM_004004.6(GJB2):c.*544T>C	rs564755659
NM_004004.6(GJB2):c.-170C>G	rs1006263046

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